PE20110560A1 - NEW DERIVATIVES OF TRIAZOLO [4,3-a] PYRIDINE, ITS PREPARATION PROCEDURE, ITS APPLICATION AS MEDICINES, PHARMACEUTICAL COMPOSITIONS AND NEW USE, PARTICULARLY AS MET INHIBITORS - Google Patents

NEW DERIVATIVES OF TRIAZOLO [4,3-a] PYRIDINE, ITS PREPARATION PROCEDURE, ITS APPLICATION AS MEDICINES, PHARMACEUTICAL COMPOSITIONS AND NEW USE, PARTICULARLY AS MET INHIBITORS

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Publication number
PE20110560A1
PE20110560A1 PE2011000048A PE2011000048A PE20110560A1 PE 20110560 A1 PE20110560 A1 PE 20110560A1 PE 2011000048 A PE2011000048 A PE 2011000048A PE 2011000048 A PE2011000048 A PE 2011000048A PE 20110560 A1 PE20110560 A1 PE 20110560A1
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Peru
Prior art keywords
triazolo
new
medicines
pyridine
pharmaceutical compositions
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Application number
PE2011000048A
Other languages
Spanish (es)
Inventor
Eric Bacque
Dominique Damour
Conception Nemecek
Patrick Nemecek
Sylvie Wentzler
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Sanofi Aventis
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Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=41550767&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PE20110560(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority claimed from FR0804084A external-priority patent/FR2933980B1/en
Priority claimed from FR0900245A external-priority patent/FR2941229B1/en
Application filed by Sanofi Aventis filed Critical Sanofi Aventis
Publication of PE20110560A1 publication Critical patent/PE20110560A1/en

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/425Thiazoles
    • A61K31/428Thiazoles condensed with carbocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
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    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
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    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
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    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
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  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
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  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
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  • Emergency Medicine (AREA)
  • Pain & Pain Management (AREA)
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  • Neurosurgery (AREA)
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  • Urology & Nephrology (AREA)
  • Dermatology (AREA)
  • Endocrinology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

REFERIDA A UN COMPUESTO DE FORMULA I, DONDE Ra ES H, HALOGENO, ARILO, HETEROARILO, HETEROARILO, ENTRE OTROS; RB ES H, ALQUILO, -COO-ALQUILO, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: N-[6-([1,2,4]TRIAZOLO[4,3-a]PIRIDIN-3-ILSULFANIL)-1,3-BENZOTIAZOL-2-IL]UREA; 6-[(6-YODO[1,2,4]TRIAZOLO[4,3-a]PIRIDIN-3-IL)SULFANIL]-1,3-BENZOTIAZOL-2-AMINA; N-(6-{[6-(1-METIL-1H-PIRAZOL-4-IL)[1,2,4]TRIAZOLO[4,3-a]PIRIDIN-3-IL]SULFANIL}-1,3-BENZOTIAZOL-2-IL)CICLOPROPANOCARBOXAMIDA; ENTRE OTROS. REFERIDA TAMBIEN A UN PROCESO DE PREPARACION Y A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE LA ACTIVIDAD DE LA PROTEINA QUINASA MET Y DE SUS FORMAS MUTANTES, UTILES EN EL TRATAMIENTO DE CANCERREFERRING TO A COMPOUND OF FORMULA I, WHERE Ra IS H, HALOGEN, ARYL, HETEROARILO, HETEROARILO, AMONG OTHERS; RB IS H, ALKYL, -COO-ALKYL, AMONG OTHERS. THE PREFERRED COMPOUNDS ARE: N- [6 - ([1,2,4] TRIAZOLO [4,3-a] PYRIDIN-3-ILSULFANIL) -1,3-BENZOTHIAZOL-2-IL] UREA; 6 - [(6-IODINE [1,2,4] TRIAZOLO [4,3-a] PYRIDIN-3-IL) SULFANIL] -1,3-BENZOTHIAZOL-2-AMINE; N- (6 - {[6- (1-METHYL-1H-PYRAZOLE-4-IL) [1,2,4] TRIAZOLO [4,3-a] PYRIDIN-3-IL] SULFANIL} -1,3- BENZOTHIAZOL-2-IL) CYCLOPROPANOCARBOXAMIDE; AMONG OTHERS. ALSO REFERRED TO A PREPARATION PROCESS AND A PHARMACEUTICAL COMPOSITION. SUCH COMPOUNDS ARE INHIBITORS OF THE ACTIVITY OF PROTEIN KINASE MET AND ITS MUTANT FORMS, USEFUL IN THE TREATMENT OF CANCER

PE2011000048A 2008-07-18 2009-07-16 NEW DERIVATIVES OF TRIAZOLO [4,3-a] PYRIDINE, ITS PREPARATION PROCEDURE, ITS APPLICATION AS MEDICINES, PHARMACEUTICAL COMPOSITIONS AND NEW USE, PARTICULARLY AS MET INHIBITORS PE20110560A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR0804084A FR2933980B1 (en) 2008-07-18 2008-07-18 NOVEL TRIAZOLO®4,3-A! PYRIDINE DERIVATIVES, PROCESS FOR THEIR PREPARATION, THEIR USE AS MEDICAMENTS, PHARMACEUTICAL COMPOSITIONS AND NOVEL USE IN PARTICULAR AS MET INHIBITORS
FR0900245A FR2941229B1 (en) 2009-01-21 2009-01-21 NOVEL TRIAZOLO®4,3-A! PYRIDINE DERIVATIVES, PROCESS FOR THEIR PREPARATION, THEIR USE AS MEDICAMENTS, PHARMACEUTICAL COMPOSITIONS AND NOVEL USE IN PARTICULAR AS MET INHIBITORS

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PE20110560A1 true PE20110560A1 (en) 2011-08-29

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PE2011000048A PE20110560A1 (en) 2008-07-18 2009-07-16 NEW DERIVATIVES OF TRIAZOLO [4,3-a] PYRIDINE, ITS PREPARATION PROCEDURE, ITS APPLICATION AS MEDICINES, PHARMACEUTICAL COMPOSITIONS AND NEW USE, PARTICULARLY AS MET INHIBITORS

Country Status (19)

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US (1) US20110263594A1 (en)
EP (1) EP2310366A2 (en)
JP (1) JP2011528337A (en)
KR (1) KR20110039558A (en)
CN (1) CN102159543A (en)
AR (1) AR072819A1 (en)
AU (1) AU2009272516A1 (en)
BR (1) BRPI0916464A2 (en)
CA (1) CA2730959A1 (en)
CL (1) CL2011000119A1 (en)
CO (1) CO6331463A2 (en)
EA (1) EA201170222A1 (en)
IL (1) IL210688A0 (en)
MA (1) MA32570B1 (en)
MX (1) MX2011000671A (en)
PE (1) PE20110560A1 (en)
TW (1) TW201008938A (en)
UY (1) UY31996A (en)
WO (1) WO2010007316A2 (en)

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US8759535B2 (en) 2010-02-18 2014-06-24 High Point Pharmaceuticals, Llc Substituted fused imidazole derivatives, pharmaceutical compositions, and methods of use thereof
FR2966151B1 (en) * 2010-10-14 2012-11-09 Sanofi Aventis 6- (ALKYL- OR CYCLOALKYL-TRIAZOLOPYRIDAZINE-SULFANYL) BENZOTHIAZOLES DERIVATIVES: PREPARATION, APPLICATION AS MEDICAMENTS AND USE AS MET INHIBITORS
WO2012116237A2 (en) * 2011-02-23 2012-08-30 Intellikine, Llc Heterocyclic compounds and uses thereof
WO2013038362A1 (en) 2011-09-15 2013-03-21 Novartis Ag 6 - substituted 3 - (quinolin- 6 - ylthio) - [1,2,4] triazolo [4, 3 -a] pyradines as tyrosine kinase
CN105143228B (en) * 2013-05-10 2017-07-21 江苏豪森药业集团有限公司 [1,2,4] triazol [4,3 a] pyridine derivatives, its preparation method or its in application pharmaceutically
US20160108039A1 (en) * 2013-06-03 2016-04-21 Bayer Pharma Aktiengesellschaft Triazolopyridines as thrombin inhibitors for the treatment of thromboembolic diseases
GB201321742D0 (en) * 2013-12-09 2014-01-22 Ucb Pharma Sa Therapeutic agents
WO2016089648A1 (en) 2014-12-01 2016-06-09 Vtv Therapeutics Llc Bach 1 inhibitors in combination with nrf2 activators and pharmaceutical compositions thereof
CN106489962B (en) * 2016-10-20 2019-02-22 贵州大学 One kind [1,2,4] triazole [4,3-a] pyridines sulfur-containing compound is preparing the application in insecticide
JP7414282B2 (en) 2017-12-07 2024-01-16 ザ リージェンツ オブ ザ ユニバーシティ オブ ミシガン NSD family inhibitors and methods of treatment using them
EA202192575A1 (en) 2019-03-21 2022-01-14 Онксео DBAIT COMPOUNDS IN COMBINATION WITH KINASE INHIBITORS FOR CANCER TREATMENT
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FR2601952B1 (en) * 1986-07-23 1988-11-25 Carpibem NOVEL AMINO ALKYL THIO DERIVATIVES OF TRIAZOLOPYRIDINE OR TRIAZOLOQUINOLINE, PROCESSES FOR THEIR PREPARATION, MEDICAMENTS CONTAINING THEM, USEFUL IN PARTICULAR AS ANTALGICS
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EP2310366A2 (en) 2011-04-20
AR072819A1 (en) 2010-09-22
US20110263594A1 (en) 2011-10-27
TW201008938A (en) 2010-03-01
JP2011528337A (en) 2011-11-17
CN102159543A (en) 2011-08-17
MX2011000671A (en) 2011-04-11
AU2009272516A1 (en) 2010-01-21
WO2010007316A3 (en) 2010-04-29
CO6331463A2 (en) 2011-10-20
CA2730959A1 (en) 2010-01-21
BRPI0916464A2 (en) 2018-06-12
EA201170222A1 (en) 2011-08-30
KR20110039558A (en) 2011-04-19
IL210688A0 (en) 2011-03-31
WO2010007316A2 (en) 2010-01-21
UY31996A (en) 2010-02-26
MA32570B1 (en) 2011-08-01
CL2011000119A1 (en) 2011-06-17

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